Takabayashi Shin, Shimpo Hideto, Yokoyama Kazuto
Department of Thoracic and Cardiovascular Surgery, Mie University Graduate School of Medicine, 2-174 Edobashi, Tsu, Mie 514-8507, Japan.
Gen Thorac Cardiovasc Surg. 2007 May;55(5):197-9. doi: 10.1007/s11748-007-0104-z.
A 6-month-old boy was diagnosed with coronary sinus orifice atresia, double-outlet right ventricle, complete atrioventricular septal defect, pulmonary stenosis, and moderate common atrioventricular valve regurgitation associated with heterotaxy syndrome. Cardiac venous flow drained through a persistent left superior vena cava. We decided to perform coronary sinus orifice unroofing through the right atrium under a guide using a bougie. The persistent left superior vena cava was divided. Bidirectional Glenn anastomosis and edge-to-edge common atrioventricular valve repair were concomitantly performed. After a 1-year follow-up period, the patient is alive and well without any ischemic event.
一名6个月大的男婴被诊断为冠状静脉窦口闭锁、右心室双出口、完全性房室间隔缺损、肺动脉狭窄以及与内脏异位综合征相关的中度共同房室瓣反流。心脏静脉血流经持续存在的左上腔静脉引流。我们决定在导丝引导下经右心房进行冠状静脉窦口开窗术。将持续存在的左上腔静脉离断。同时进行双向格林吻合术和共同房室瓣的缘对缘修复。经过1年的随访期,患者存活且状况良好,未发生任何缺血事件。